Summary
The FDA issued a Class II for Recreo Hair Growth Laser Comb by OMM Imports, Inc. dba Zero Gravity. Reason: The firm distributed the laser products without affixing the warning, aperture, certification, and identification labels. In addition, the firm failed.
Details
Source
Device Recall
External ID
Z-1222-2023
Action Date
2023-03-22
Status
Ongoing
Category
device
Product Description
Recreo Hair Growth Laser Comb
Lot/Code Info: Class 3R Zero Gravity Recreo Hair Growth Laser Comb
Quantity Affected: 1620 units shipped to United States
Reason for Recall
The firm distributed the laser products without affixing the warning, aperture, certification, and identification labels. In addition, the firm failed to provide safety information, reproductions and locations of the labels, and a warning statement in the user manual.
Distribution
Worldwide and Nationwide including DC and Puerto Rico
Type: Voluntary: Firm initiated
Recall Initiated: 2022-09-01
Company
Miami Beach, FL
Context & Analysis
This is a Class II recall. Class II recalls indicate that use of or exposure to the product may cause temporary or medically reversible health consequences, or that the probability of serious consequences is remote.
This was one of 134 device recalls issued in the same week, part of 403 device-related FDA actions this month.
Frequently Asked Questions
What is a Class II recall?
A Class II recall means the product may cause temporary or medically reversible adverse health consequences, or the probability of serious adverse consequences is remote. Consumers should discontinue use.
What should I do if I have this product?
Stop using the product. Check the product against the specific lot numbers or identifiers listed in the recall. Contact the manufacturer (OMM Imports, Inc. dba Zero Gravity) or your retailer for a refund or replacement. If you experienced adverse effects, report them to the FDA via MedWatch.
How often does OMM Imports, Inc. dba Zero Gravity have FDA actions?
This is the only FDA action we have on record for OMM Imports, Inc. dba Zero Gravity in our database.
Where can I find the official FDA record?
The official record is available on FDA.gov. Search for "Z-1222-2023" on FDA.gov for the full record. You can also use the openFDA API to query this record programmatically.
Want to know the moment something like this happens?
Get alerts for deviceRelated Actions
MAHURKAR 12 Fr High Pressure Triple Lumen Acute Dialysis Catheter, 24 cm, Straight Extensions, IC Tray REF: 888810200
Covidien LP · 2023-08-23
Sterile Procedural Trays, labeled as the following: a. BREAST AUGMENTATION b. BREAST REDUCTION CDS c. CUH ABDOMINO
MEDLINE INDUSTRIES, LP - Northfield · 2023-02-15
VTC Regular Kit Nephrostomy Catheter System Kit, Material Number REF M001245300; to provide external drainage of the uri
Boston Scientific Corporation · 2024-09-25
EnChroma Safety Glasses with Rx Indoor Universal Lenses: Martinez Cx1 Indoor Rx, SKU: Cx.PC.IN.MTZ.BK.Rx; Summit Indoo
Enchroma Inc · 2024-11-27
Otological Ventilation Tube - T-Tube 9mm - Silicone; Product Code: NZ3309;
Adept Medical Ltd · 2025-01-29